**Educational Website Text:**---**13. Reaction Pathway: Compound Transformation**- **Objective:** Outline the steps required to convert the compound on the left to the compound on the right.- **Structures:** - **Left Compound:** An ester with a methyl group (CH₃) attached to a carbonyl (C=O) leading to a five-carbon chain. - **Right Compound:** An alcohol with a six-carbon chain, maintaining a terminal carbonyl group (C=O).- **Diagram Description:** - The transformation involves modifying functional groups and chain length.---**14. Synthesis Mechanism: Williamson Ether Synthesis**- **Objective:** Detail the steps necessary to synthesize the compound known as phenyl propyl ether through Williamson ether synthesis.- **Target Compound:** Phenyl propyl ether- This classic synthesis method involves reacting an alkoxide ion with a primary alkyl halide under basic conditions to form ethers.---

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13. Show the steps necessary to transform the compound on the left into the compound on the right. HO H. 14 Show the steps necessary to synthesize this compound by the Williamson ether synthesis. → phenyl propyl ether

13. Show the steps necessary to transform the compound on the left into the compound on the right. HO H. 14 Show the steps necessary to synthesize this compound by the Williamson ether synthesis. → phenyl propyl ether

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

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Concept explainers

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.

Question

**Educational Website Text:**

---

**13. Reaction Pathway: Compound Transformation**

- **Objective:** Outline the steps required to convert the compound on the left to the compound on the right.

- **Structures:**
- **Left Compound:** An ester with a methyl group (CH₃) attached to a carbonyl (C=O) leading to a five-carbon chain.
- **Right Compound:** An alcohol with a six-carbon chain, maintaining a terminal carbonyl group (C=O).

- **Diagram Description:**
- The transformation involves modifying functional groups and chain length.

---

**14. Synthesis Mechanism: Williamson Ether Synthesis**

- **Objective:** Detail the steps necessary to synthesize the compound known as phenyl propyl ether through Williamson ether synthesis.

- **Target Compound:** Phenyl propyl ether

- This classic synthesis method involves reacting an alkoxide ion with a primary alkyl halide under basic conditions to form ethers.

---

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